CAS 1116-22-9

L-γ-Glutamyl-L-glutamic acid

Description:

L-γ-Glutamyl-L-glutamic acid, also known as a dipeptide, is a compound formed from two glutamic acid residues linked by a peptide bond. It is characterized by its structure, which includes a carboxylic acid functional group and an amine group, typical of amino acids. This substance is soluble in water, reflecting the polar nature of its functional groups, and it exhibits properties associated with amino acids, such as the ability to participate in various biochemical reactions. L-γ-Glutamyl-L-glutamic acid is often studied in the context of its role in metabolic pathways and its potential applications in nutrition and pharmaceuticals. It may also exhibit biological activity, influencing neurotransmission and cellular signaling due to its involvement in the synthesis of neurotransmitters. The compound's stability and reactivity can be influenced by factors such as pH and temperature, making it important to consider these conditions in experimental settings. Overall, L-γ-Glutamyl-L-glutamic acid is a significant molecule in biochemistry with various implications in health and disease.

Formula: C₁₀H₁₆N₂O₇

InChI: InChI=1S/C10H16N2O7/c11-5(9(16)17)1-3-7(13)12-6(10(18)19)2-4-8(14)15/h5-6H,1-4,11H2,(H,12,13)(H,14,15)(H,16,17)(H,18,19)/t5-,6-/m0/s1

InChI key: InChIKey=OWQDWQKWSLFFFR-WDSKDSINSA-N

SMILES: [C@H](NC(CC[C@@H](C(O)=O)N)=O)(CCC(O)=O)C(O)=O

Synonyms:

• (2S)-2-{[(4S)-4-ammonio-4-carboxylatobutanoyl]amino}pentanedioate
• <span class="text-smallcaps">L</smallcap>-Glutamic acid, <smallcap>L</span>-γ-glutamyl-
• <span class="text-smallcaps">L</smallcap>-Glutamic acid, N-<smallcap>L</span>-γ-glutamyl-
• <span class="text-smallcaps">L</smallcap>-γ-Glutamyl-<smallcap>L</span>-glutamic acid
• Gamma-Glutamylglutamic Acid
• Glutamic acid, N-<span class="text-smallcaps">L</smallcap>-γ-glutamyl-, <smallcap>L</span>-
• Glutamic acid, N-<span class="text-smallcaps">L</span>-γ-glutamyl-
• H-Gamma-Glu-Glu-Oh
• L-gamma-glutamyl-L-glutamic acid
• N-gamma-L-Glutamyl-L-glutamic acid
• gamma-Glutamylglutamate
• γ-<span class="text-smallcaps">L</smallcap>-Glutamyl-<smallcap>L</span>-glutamic acid
• γ-Glutamylglutamic acid
• L-Glutamic acid, N-L-γ-glutamyl-
• L-Glutamic acid, L-γ-glutamyl-
• Glutamic acid, N-L-γ-glutamyl-
• Glutamic acid, N-L-γ-glutamyl-, L-

H-Glu(Glu-OH)-OH

CAS: 1116-22-9

Bachem ID: 4000639.

Formula: C₁₀H₁₆N₂O₇

Color and Shape: White Powder

Molecular weight: 276.25

Ref: 01-4000639

H-γ-Glu-Glu-OH

CAS: 1116-22-9

Formula: C₁₀H₁₆N₂O₇

Purity: 95%

Color and Shape: Solid

Molecular weight: 276.2432

Ref: IN-DA0079ES

L-γ-Glutamyl-L-glutamic acid

CAS: 1116-22-9

L-γ-Glutamyl-L-glutamic acid

Purity: 98%

Ref: 54-OR1037145

Glutamic Acid Impurity 1

CAS: 1116-22-9

Formula: C₁₀H₁₆N₂O₇

Molecular weight: 276.25

Ref: 4Z-PG-356

γ-L-Glutamyl L-Glutamic Acid

Controlled Product

CAS: 1116-22-9

Applications H-GAMMA-GLU-GLU-OH (cas# 1116-22-9) is a useful research chemical.

Formula: C₁₀H₁₆N₂O₇

Color and Shape: Neat

Molecular weight: 276.24

Ref: TR-G245125

H-Glu(Glu-OH)-OH

CAS: 1116-22-9

H-Glu(Glu-OH)-OH is a synthetic amino acid that is currently being investigated as a diagnostic agent for the detection of intracellular protein degradation by matrix metalloproteinase-9 (MMP-9). H-Glu(Glu-OH)-OH is taken up by cells in a concentration and time dependent manner, with an uptake rate of approximately 1.6 x 10^6 molecules per cell per hour. The uptake mechanism is not yet known, but has been hypothesized to be due to receptor binding. H-Glu(Glu-OH)-OH binds to cerebellar granule cells and alters mitochondrial metabolism, which may be related to its effects on the ubiquitin proteasome pathway. This compound also has diagnostic potential for atherosclerosis and glutamate transport disorders.

Formula: C₁₀H₁₆N₂O₇

Purity: Min. 95%

Molecular weight: 276.24 g/mol

Ref: 3D-FG108030